CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 737 enrolled
Drug / intervention
Dulaglutide +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01644500
NCT01644500Phase 3Completed

The Efficacy and Safety of Once-Weekly, Subcutaneous Dulaglutide Monotherapy Compared to Glimepiride in Patients With Type 2 Diabetes Mellitus

Eli Lilly and Company·interventional·Posted Jul 19, 2012·Updated Sep 18, 2019

In Brief

A Phase 3 clinical trial evaluating Dulaglutide, Glimepiride, and 2 other interventions for Type 2 Diabetes Mellitus. Completed, enrolled 737 participants across 30 sites in 3 countries.

Detailed Summary

The purpose of this study is to examine if once-weekly dulaglutide is efficient and safe compared to glimepiride in participants with type 2 diabetes mellitus who have inadequate glycemic control with oral antihyperglycemic medication (OAM) or are OAM-naïve.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina, South Korea, Taiwan
Collaborators--

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJul 19, 2012
Enrollment StartJul 1, 2012
Primary CompletionAug 1, 2014
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 14.0 years ago

Interventions

Dulaglutidedrug

Administered SC

Glimepiridedrug

Administered orally

Placebo as Capsulesdrug

Placebo for glimepiride is administered orally as one to three capsules daily.

Placebo as SC Injectiondrug

Placebo for dulaglutide is administered as one SC injection.